All individuals with variants in gene HMGA2

11 entries on 1 page. Showing entries 1 - 11.
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00080114 19762329-PatSR29 PubMed: Spengler 2010, for EUCID-SRS consortium - F - - - - - - - SRS;RSS prominent forehead (HP:0011220) 1 1 Zeynep Tümer
00117196 25809938-PatII3 PubMed: De Crescenzo 2015, for EUCID-SRS consortium 3-generation family, 4 affecteds (3F, M), mother II3 F - Italy - - - - - SRS;RSS prominent forehead (HP:0011220) 1 4 Zeynep Tümer
00117197 25809938-PatIII1 PubMed: De Crescenzo 2015, for EUCID-SRS consortium daughter III1 F - Italy - - - - - SRS;RSS prominent forehead (HP:0011220) 1 1 Zeynep Tümer
00117198 28796236-Pat PubMed: Abi Habib 2017, for EUCID-SRS consortium - - - - - - - - - SRS;RSS prominent forehead (HP:0011220) 1 1 Zeynep Tümer
00117199 28796236-Pat PubMed: Abi Habib 2017, for EUCID-SRS consortium - - - - - - - - - SRS;RSS prominent forehead (HP:0011220) 1 1 Zeynep Tümer
00154495 - - - F no Germany - 04y - - - SRS;RSS see paper; ..., triangular face (HP:0000325) 1 1 Matias Wagner
00412476 B.II-1 PubMed: Delvallee 2021 - - - France - - - - - retinal disease sensorineural features: retinal dystrophy, nystagmus; abnormalities of the hands and feet: postaxial polydactyly: hands; brachydactyly; obesity: BMI (47.3); mild intellectual disability; learning difficulty; slow ideation; motor development delay; micropenis; cryptorchidism 1 1 LOVD
00449692 - - - F no Japan - - - - - SRS;RSS Triangular face, Micrognathia, Clinodactyly; prominent forehead (HP:0011220) 1 1 Kaori Yamoto
00449693 - - - M no Japan - - - - - SRS;RSS see paper; ..., triangular face, micrognathia, clinodactyly, osteopoikilosis; no prominent forehead (-HP:0011220) 1 1 Kaori Yamoto
00466039 314C - - M - Hong Kong Chinese - - - - ADHD - 1 1 Larry Baum
00466693 Pat14 PubMed: Plachy 2019 - M - Czech Republic - - - - - stature, short see paper; ..., growth hormone deficiency; height SDS-3.06; birth weight SDS-1.94, length SDS-1.42 1 1 Johan den Dunnen
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